Canonical Allele Identifier: CA74631931

Gene: ZMYND10

Linked Data

• dbSNP Id: rs982314943
• gnomAD v3: 3-50342796-C-A
• gnomAD v4: 3-50342796-C-A
• MyVariant Identifiers: chr3:g.50380227C>A (hg19) ; chr3:g.50342796C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50342796C>A , CM000665.2:g.50342796C>A	GRCh38
NC_000003.11:g.50380227C>A , CM000665.1:g.50380227C>A	GRCh37
NC_000003.10:g.50355231C>A	NCBI36
NG_023270.1:g.3141G>T
NG_042828.1:g.7951G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231749.8:c.700+122G>T MANE Select	ENSP00000231749.3:n.700+122G>T
ENST00000231749.7:c.700+122G>T	ENSP00000231749.3:n.700+122G>T
ENST00000360165.7:c.600-141G>T	ENSP00000353289.3:n.600-141G>T
ENST00000442887.1:c.571+122G>T	ENSP00000393687.1:n.571+122G>T
ENST00000443080.5:c.*452+122G>T	ENSP00000415661.1:n.*452+122G>T
ENST00000475688.1:n.373G>T
NM_001308379.1:c.600-141G>T	NP_001295308.1:n.600-141G>T
NM_015896.2:c.700+122G>T	NP_056980.2:n.700+122G>T
NM_015896.3:c.700+122G>T	NP_056980.2:n.700+122G>T
XM_005265216.2:c.463+122G>T	XP_005265273.1:n.463+122G>T
XM_005265216.3:c.463+122G>T	XP_005265273.1:n.463+122G>T
NM_015896.4:c.700+122G>T MANE Select	NP_056980.2:n.700+122G>T
NM_001308379.2:c.600-141G>T	NP_001295308.1:n.600-141G>T